(4Z,6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26E,28Z)-2,31-dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-4,6,8,10,12,14,16,18,20,22,24,26,28-tridecaene

Details

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Internal ID 2fa55455-4f4e-49bb-aca1-9b1b769803d6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Xanthophylls
IUPAC Name (4Z,6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26E,28Z)-2,31-dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-4,6,8,10,12,14,16,18,20,22,24,26,28-tridecaene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H60O2/c1-35(23-15-25-37(3)27-17-29-39(5)31-19-33-41(7,8)43-11)21-13-14-22-36(2)24-16-26-38(4)28-18-30-40(6)32-20-34-42(9,10)44-12/h13-32H,33-34H2,1-12H3/b14-13+,23-15+,24-16+,27-17+,28-18+,31-19-,32-20-,35-21+,36-22+,37-25+,38-26+,39-29+,40-30+
InChI Key VAZQBTJCYODOSV-FLOSMPHISA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C42H60O2
Molecular Weight 596.90 g/mol
Exact Mass 596.45933115 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 13.90
Atomic LogP (AlogP) 12.19
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 18

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4Z,6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26E,28Z)-2,31-dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-4,6,8,10,12,14,16,18,20,22,24,26,28-tridecaene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 - 0.8026 80.26%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.4949 49.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8554 85.54%
OATP1B3 inhibitior + 0.9318 93.18%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9969 99.69%
P-glycoprotein inhibitior + 0.8045 80.45%
P-glycoprotein substrate - 0.8926 89.26%
CYP3A4 substrate - 0.5126 51.26%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.7504 75.04%
CYP3A4 inhibition - 0.8863 88.63%
CYP2C9 inhibition - 0.8768 87.68%
CYP2C19 inhibition - 0.7421 74.21%
CYP2D6 inhibition - 0.9269 92.69%
CYP1A2 inhibition - 0.8582 85.82%
CYP2C8 inhibition - 0.8837 88.37%
CYP inhibitory promiscuity - 0.6937 69.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5983 59.83%
Carcinogenicity (trinary) Non-required 0.4829 48.29%
Eye corrosion - 0.6927 69.27%
Eye irritation - 0.8761 87.61%
Skin irritation + 0.7687 76.87%
Skin corrosion - 0.9924 99.24%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9241 92.41%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5419 54.19%
skin sensitisation + 0.8964 89.64%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.7019 70.19%
Acute Oral Toxicity (c) III 0.7238 72.38%
Estrogen receptor binding + 0.8040 80.40%
Androgen receptor binding - 0.7104 71.04%
Thyroid receptor binding + 0.7396 73.96%
Glucocorticoid receptor binding + 0.7141 71.41%
Aromatase binding - 0.5193 51.93%
PPAR gamma + 0.7611 76.11%
Honey bee toxicity - 0.8071 80.71%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity - 0.4294 42.94%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.53% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.39% 89.34%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.07% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.98% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.75% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.58% 96.95%
CHEMBL1870 P28702 Retinoid X receptor beta 81.26% 95.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.60% 99.17%
CHEMBL2581 P07339 Cathepsin D 80.59% 98.95%
CHEMBL2061 P19793 Retinoid X receptor alpha 80.46% 91.67%
CHEMBL2004 P48443 Retinoid X receptor gamma 80.10% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 9873404
LOTUS LTS0176813
wikiData Q105283106